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Overview of included studies for HSP-SPAST:
Click here for summary of patients' characteristics
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Filter for
all included patients
index patients only
AAO < 50 (adjustable)
AAO >= 50 (adjustable)
females only
males only
homozygous only
heterozygous only
compound heterozygous only
homozygous and compound heterozygous
carrying
definitely pathogenic mutations
probably pathogenic mutations
possibly pathogenic mutations
c.(1098+1+1099-1)_(1493+1_1494-1)del
c.(1098+1_1099-1)_(3149_?)del
c.(1098+1_1099-1)_(1173+1_1174-1)del
c.(1098+1_1099-1)_(1245+1_1246-1)del
c.(1173+1_1174-1)_(3149_?)del
c.(1173+1_1174-1)_(1245+1_1246-1)del
c.(1173+1_1174-1)_(1493+1_1494-1)del
c.(1245+1_1246-1)_(3149_?)del
c.(1245+1_1246-1)_(1321+1_1322-1)del
c.(1245+1_1246-1)_(1493+1_1494-1)del
c.(1245+1_1246-1)_(1728+1_1729-1)del
c.(1245+1_1246-1)_(1728+1_1729-1)dup
c.(1493+1_1494-1)_(1536+1_1537-1)del
c.(1493+1_1494-1)_(1728+1_1729-1)del
c.(1536+1_1537-1)_(1687+1_1688-1)dup
c.(1536+1_1537-1)_(1728+1_1729-1)del
c.(1687+1_1688-1)_(3149_?)del
c.(1687+1_1688-1)_(1728+1_1729-1)del
c.(1687+1_1688-1)_(1728+1_1729-1)dup
c.(1728+1_1729-1)_(3149_?)del
c.(415+1_416-1)_(3149_?)del
c.(415+1_416-1)_(1245+1_1246-1)del
c.(415+1_416-1)_(1493+1_1494-1)dup
c.(415+1_416-1)_(1728+1_1729-1)del
c.(586+1_587-1)_(3149_?)del
c.(586+1_587-1)_(1098+1_1099-1)del
c.(586+1_587-1)_(1245+1_1246-1)del
c.(682+1_683-1)_(3149_?)del
c.(682+1_683-1)_(1004+1_1005-1)del
c.(682+1_683-1)_(1098+1_1099-1)del
c.(682+1_683-1)_(870+1_871-1)del
c.(870+1_871-1)_(1004+1_1005-1)del
c.(870+1_871-1)_(1098+1_1099-1)del
c.(?_-221)_(3149_?)del
c.(?_-221)_(1245+1_1246-1)del
c.(?_-221)_(415+1_416-1)del
c.(?_-221)_(415+1_416-1)dup
c.(?_-221)_(502+1_503-1)del
c.(?_-221)_(586+1_587-1)del
c.(?_-221)_(682+1_683-1)del
c.1-763_c.683-650del
c.1004+1G>T
c.1004+2T>A
c.1004+2T>G
c.1004+3A>C
c.1004+5G>C
c.1005-1G>A
c.1005-1G>C
c.1005-2A>G
c.1014delT
c.1024G>C
c.1031T>A
c.1036G>T
c.1039C>A
c.1039C>T
c.1040A>C
c.1048G>C
c.1054C>T
c.1055A>C
c.1067A>G
c.1070T>A
c.1072G>C
c.1078C>G
c.1079T>C
c.1081C>A
c.1081C>T
c.1082C>G
c.1082C>T
c.1088T>C
c.1091G>C
c.1092_1098+1delGCCTGAGG
c.1096G>A
c.1098+1G>A
c.1098+1G>C
c.1098+1_1098+2delinsCTCAGA
c.1099-1G>A
c.1099-2_1099delAGT
c.1100T>C
c.1101_1103delGTT
c.1103T>C
c.1105A>C
c.1105dupA
c.1108G>A
c.1111C>T
c.1114A>G
c.1120C>A
c.1121C>G
c.1128A>C
c.1133T>A
c.1133T>C
c.1136dupT
c.1137_1142delACTCTT
c.1137dupA
c.1139T>A
c.1141T>C
c.1151C>G
c.1153G>T
c.1154G>A
c.1158T>G
c.1160_1170del11
c.1163A>G
c.1165A>G
c.1167_1168delAA
c.1168A>G
c.1172T>C
c.1173+1G>A
c.1174-1G>A
c.1174-1G>C
c.1174-1G>T
c.1174-1_1174delinsCT
c.1174_1180delGCTAAAG
c.1174delG
c.1176dupT
c.1177_1188del12
c.1180delG
c.1185delA
c.1192_1193delinsT
c.1196C>T
c.1209C>A
c.1209C>G
c.1209_1211delCTT
c.1210_1212delTTT
c.1215_1219delTATAA
c.1215dupT
c.1216A>G
c.1217T>G
c.1225G>A
c.1226C>A
c.1238C>T
c.1242A>G
c.1243_1244insA
c.1244dupA
c.1245+1G>A
c.1245+1G>T
c.1245+3insT
c.1245+4A>G
c.1245+5G>A
c.1245delC
c.1246-1G>C
c.1246-2896_1493+523dup
c.1246-4_1246-2delinsCT
c.1250G>A
c.1251_1253delAGA
c.1253_1255delAAG
c.1255G>T
c.1267G>T
c.1270A>G
c.1270_1271dupAG
c.1276C>G
c.1276C>T
c.1276_1277delCT
c.127G>T
c.1280T>G
c.1281delT
c.1281dupT
c.1282G>C
c.1282delG
c.1291C>T
c.1300C>T
c.1304C>T
c.1306T>C
c.1307C>T
c.1317delT
c.131C>A
c.131C>T
c.1321+2T>A
c.1321G>A
c.1322-2A>C
c.1322-2A>G
c.1322A>G
c.1322A>T
c.1322_31del29
c.1324G>A
c.1324G>T
c.1325A>C
c.1326_1331delAGTTGA
c.1330G>A
c.1331A>G
c.1332T>G
c.1334G>C
c.1339T>G
c.1340delT
c.1341_1342insTC
c.134C>A
c.1350_1351delAA
c.1352_1356delGAGAA
c.1353_1357delAGAAG
c.1355_1357delAAG
c.1356delA
c.1358_1360dupGGG
c.1360G>A
c.1361A>G
c.1375A>G
c.1376G>C
c.1378C>A
c.1378C>T
c.1379G>A
c.1379G>T
c.1379delG
c.1382T>C
c.1384A>G
c.1385A>G
c.1387A>G
c.1392A>T
c.139A>T
c.1402G>T
c.1408G>T
c.1409A>T
c.1412G>A
c.1413+1G>A
c.1413+2T>A
c.1413+2T>G
c.1413+3A>C
c.1413+3_1413+6delAAGT
c.1413+4A>G
c.1413+5G>A
c.1413+6T>C
c.1413dupT
c.1414-1G>A
c.1414-1G>C
c.1414-2A>C
c.1414-2A>G
c.1414G>A
c.1417C>T
c.1418_1431del14
c.1426_1427delGG
c.1435_1441delAGAGTAC
c.1437_1438delAG
c.1439_1445delinsC
c.1442_1443insA
c.1447_1448delAT
c.1450G>C
c.1450_1458delGGTGCAACT
c.1454C>T
c.1459A>C
c.1459A>G
c.1461_1462dupTA
c.1466C>G
c.1466C>T
c.1468C>T
c.1474C>T
c.1478A>G
c.1492A>G
c.1492_1493+2delAGGT
c.1493+1G>A
c.1493+1_1493+2insATGG
c.1493+2T>C
c.1493+2_1493+5delTAGG
c.1493G>C
c.1494-2A>G
c.1494G>T
c.1495C>T
c.1496G>A
c.1504A>T
c.1507C>T
c.1507_1509dupCGG
c.1511dupT
c.1512_1514dupATA
c.1517T>A
c.1517T>G
c.1520_1521dupCT
c.1529A>T
c.1535delA
c.1536+1G>A
c.1536+1G>T
c.1540A>G
c.1543_1545delCTA
c.1555A>T
c.155A>G
c.1560_1563delTCTG
c.1573C>T
c.1597G>T
c.1601T>C
c.1601_1608delins30
c.1608_1615delACTTGCTA
c.1610T>C
c.1610T>G
c.1616+1G>A
c.1617-1G>A
c.1617-1G>T
c.1617-2A>G
c.1625A>G
c.1630_1643del14
c.1634C>T
c.1635_1636insAA
c.1636G>A
c.1642G>A
c.1644_1649dupCCTAAC
c.1646T>C
c.1646dupT
c.1649C>T
c.1650_1651delAG
c.1651G>C
c.1656_1664delinsTGACCT
c.1664A>G
c.1666G>A
c.1667C>T
c.1667_1668delCA
c.1670C>T
c.1673T>G
c.1675G>C
c.1676G>A
c.1676insG
c.1684C>T
c.1685G>A
c.1687+1G>A
c.1687+1G>T
c.1687+2T>G
c.1687+2_1687+6delTAGGT
c.1687G>A
c.1688-2A>G
c.1688-3C>G
c.1688–1G>C
c.1689_1698del10
c.1691delT
c.1702C>T
c.1708_1716delAAGAATATG
c.1714_1715delAT
c.1724G>T
c.1728+1G>A
c.1728+1G>C
c.1728+1G>T
c.1728+2T>C
c.1728+2T>G
c.1729-1G>C
c.1729-2A>G
c.1729-2A>T
c.1732A>T
c.1735A>C
c.1738_1740delinsGA
c.1739T>C
c.1741C>T
c.1750G>C
c.1751A>T
c.1771A>G
c.1774delA
c.1776_1780delAAAAC
c.1779dupA
c.1783A>C
c.1789A>G
c.1805_1808dupAAGC
c.1812dupC
c.1815dupA
c.1821G>A
c.1821G>C
c.1837G>C
c.1838A>C
c.1838A>G
c.1840dupA
c.1841C>T
c.1841_1842delCC
c.1849T>G
c.194G>A
c.283G>A
c.283_323del41
c.286delG
c.289C>A
c.313_320delCCGGCGCC
c.334G>A
c.334G>T
c.343_352del10
c.343_352dup10
c.349C>T
c.373G>T
c.382delT
c.403G>T
c.412A>T
c.415+1G>A
c.415+1G>T
c.421C>T
c.422_425delAGAA
c.427dupG
c.439G>T
c.443G>A
c.444G>A
c.448_451delAAGA
c.450_451delGA
c.451_454delAAAG
c.458delT
c.469delG
c.484G>A
c.486dupT
c.499C>T
c.513_514delTG
c.524_525dupGA
c.532C>T
c.549dupT
c.562delG
c.571delC
c.577C>T
c.583C>G
c.584_585delTA
c.586+9_586+12delTAAT
c.602T>A
c.629_682+22003delinsAGT
c.67_85dup19
c.683-1G>A
c.683-1G>T
c.703dupA
c.706_710delAAAGA
c.712C>A
c.727_737del11
c.730_731insT
c.732_733insCA
c.734C>G
c.746C>G
c.751dupA
c.781dupT
c.782C>G
c.807C>A
c.807C>G
c.80_98dup19
c.838C>T
c.839_840delAG
c.843_846dupATCT
c.857_859delCTA
c.85dupC
c.867_868delTA
c.868A>T
c.870+1G>A
c.870+1delG
c.870+3A>G
c.871-2A>G
c.871delG
c.872_875delinsCCA
c.878C>T
c.879delG
c.906delT
c.90_91insAGCC
c.913_923delins11
c.926G>A
c.932_938delAAAAAGA
c.936_937insA
c.936dupA
c.937delG
c.941T>C
c.945delG
c.961dupG
c.96C>G
c.977dupA
c.983_984dupTA
c.990_993delTGAA
Country
Armenia
Australia
Austria
Brazil
Bulgaria
Canada
China
Czech Republic
Denmark
Estonia
France
Germany
Greece
Hungary
Ireland
Italy
Japan
Netherlands
Norway
Poland
Portugal
Russia
South Korea
Spain
Taiwan
Tunisia
Turkey
United Kingdom
United States
Study
Study design
N cases
Ethnicities
Sex
(%
♂
)
Mean AAO (+/- SD)
Reported mutations
Murphy, 2009
Family study
6
C
67%
44(+/-17)
c.(1728+1_1729-1)_(*3149_?)del
: het
Boukhris, 2009
Other/Mixed
4
B
50%
n.a.
p.Arg499Cys
: het
Svenstrup, 2009
Case report/Case series
16
C
n.a.
40(+/-15)
c.870+3A>G
: het
p.Lys393*
: het
p.Leu379Phefs*15
: het
p.Ala32Ala
: het
p.Pro34Leufs*20
: het
p.Arg364Thr
: het
c.1098+1G>A
: het
p.Ile406Val
: het
p.Arg562Gln
: het
c.1245+1G>A
: het
c.1246-1G>C
: het
p.Arg431*
: het
p.Arg499Cys
: het
c.(?_-221)_(415+1_416-1)del
: het
Show more (+11)
Scuderi, 2009
Other/Mixed
11
n.a.
55%
26(+/-24)
p.Asn405Lysfs*36
: het
p.Arg581*
: het
Shoukier, 2009
Mutational screen
47
n.a.
n.a.
n.a.
p.Gln167*
: het
p.Asn184*
: het
p.Met329*
: het
p.Pro361Ser
: het
p.Leu367Cysfs*29
: het
p.Leu367del
: het
p.Gly385Glu
: het
c.1174-1G>T
: het
p.Tyr415*
: het
p.Gly417Glu
: het
p.Phe427Cys
: het
p.Leu447Val
: het
p.Arg460His
: het
p.Gln473*
: het
p.Arg488Ilefs*43
: het
p.Leu549_Thr550dup
: het
p.Asp555Gly
: het
p.Ala557Val
: het
c.(415+1_416-1)_(1245+1_1246-1)del
: het
c.(1098+1_1099-1)_(1173+1_1174-1)del
: het
c.(1173+1_1174-1)_(*3149_?)del
: het
p.Gln125*
: het
p.Gln280Argfs*10
: het
p.Glu356Gly
: het
p.Ser399Leu
: het
p.Asn405lysfs*36
: het
p.Arg431*
: het
p.Arg562*
: het
p.Ile406Val
: het
c.1245+1G>A
: het
p.Phe427Leufs*11
: het
p.Arg460Cys
: het
p.Arg499Cys
: het
p.Arg499His
: het
p.Arg503Trp
: het
p.Trp607Cys
: het
c.(?_-221)_(586+1_587-1)del
: het
c.(415+1_416-1)_(1728+1_1729-1)del
: het
c.(1728+1_1729-1)_(*3149_?)del
: het
Show more (+36)
Loureiro, 2009
Other/Mixed
14
C
83%
31(+/-18)
p.Tyr269*
: het
p.Ser243Alafs*19
: het
c.1004+5G>C
: het
p.Gln352Pro
: het
p.Gly370Arg
: het
p.Gly387Alafs*3
: het
p.Glu454Serfs*8
: het
p.Arg460Profs*2
: het
p.Val472Cysfs*7
: het
p.Gln473*
: het
p.Lys519*
: het
p.Gln525*
: het
Show more (+9)
Orlacchio, 2008
Family study
1
C
n.a.
n.a.
p.Asp321Glyfs*6
: het
Pantakani, 2008
Other/Mixed
1
C
0%
n.a.
p.Glu563Lys
+
p.Ser44Leu
: comp. het.
Vergouwen, 2008
Case report/Case series
1
n.a.
100%
n.a.
p.Lys138*
: het
Ribaï, 2008
Other/Mixed
13
n.a.
46%
8(+/-17)
p.Arg499Cys
: het
p.Glu442Lys
: het
p.Arg459Thr
: het
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